计算机科学
蛋白质结构预测
一般化
蛋白质设计
人工智能
钥匙(锁)
序列(生物学)
蛋白质折叠
折叠(DSP实现)
桥(图论)
蛋白质结构
计算生物学
计算模型
桥接(联网)
数据科学
蛋白质工程
作者
Wanqing Yang,Yanwei Wang,Yang Wang
摘要
This systematic review outlines pivotal advancements in deep learning-driven protein structure prediction and design, focusing on four core models—AlphaFold, RoseTTAFold, RFDiffusion, and ProteinMPNN—developed by 2024 Nobel Laureates in Chemistry: David Baker, Demis Hassabis, and John Jumper. We analyze their technological iterations and collaborative design paradigms, emphasizing breakthroughs in atomic-level structural accuracy, functional protein engineering, and modeling multi-component biomolecular interactions. Key innovations include AlphaFold3's diffusion-based framework for unified biomolecular prediction, RoseTTAFold's three-track architecture integrating sequence and spatial constraints, RFDiffusion's denoising diffusion for de novo protein generation, and ProteinMPNN's inverse folding for sequence–structure co-optimization. Despite major progress in applications such as binder design, nanomaterials, and enzyme engineering, challenges persist in dynamic conformational sampling, multimodal data integration, and generalization to non-canonical targets. We propose future directions, including hybrid physics-AI frameworks and multimodal learning, to bridge gaps between computational design and functional validation in cellular environments.
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